Eleftherios Spartalis, Dimitrios I Athanasiadis, Dimosthenis Chrysikos, Michael Spartalis, Georgios Boutzios, Dimitrios Schizas, Nikolaos Garmpis, Christos Damaskos, Stavroula A Paschou, Argyrios Ioannidis, Gerasimos Tsourouflis, Dimitrios Dimitroulis, Nikolaos I Nikiteas
Journal: Anticancer research 2019;39(3):1119-1127
PMID: 30842140
BACKGROUND/AIM
Anaplastic thyroid cancer (ATC) is one of the most aggressive human malignancies, remaining generally incurable. Histone deacetylase (HDAC) seems to play a role in regulating transcription of genes involved in ATC, making HDAC inhibitors (HDACI) promising anticancer drugs for ATC. The purpose of this review was to evaluate the role of HDACIs in ATC treatment and describe the latest trends of current research on this field.
MATERIALS AND METHODS
This literature review was performed using the MEDLINE database. The keywords/phrases were; thyroid cancer, anaplastic, HDAC, histone, deacetylase*, HDACI.
RESULTS
Compounds, such as SuberoylAnilide Hydroxamic Acid, valproic acid, sodium butyrate, butyrate, phenylbutyrate, trichostatin A, AB1-13, panobinostat or LBH589, belinostat, MS-275, depsipeptide, CUDC101, CUDC907, N-Hydroxy-7-(2-naphthylthio)-Hepanomide (HNHA), and PXD101 have shown promising antitumor effects against ATC.
CONCLUSION
HDACIs represent a promising therapy for ATC management, both as monotherapy and in combination with other anticancer drugs.
Copyright© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.
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